Jha Rohan, Chalif Joshua I, Lu Yi
Neurosurgery, Harvard Medical School, Boston, USA.
Neurosurgery, Brigham and Women's Hospital, Boston, USA.
Cureus. 2024 May 20;16(5):e60694. doi: 10.7759/cureus.60694. eCollection 2024 May.
Background Suboccipital craniectomy (SOC) in conjunction with dura opening and duraplasty for posterior fossa decompression is an effective treatment for symptomatic Chiari 1 malformations (CM1), primarily carried out in the pediatric population. However, dural opening and reconstruction are associated with an increased risk of complications, and their necessity in the adult population has not yet been robustly demonstrated. Given differences in clinical presentation and disease severity between the pediatric and adult patients, we aimed to identify if SOC alone with intraoperative ultrasound confirmation of adequate restoration of pulsatile motion of cerebellar tonsil is sufficient to treat symptomatic CM1 while mitigating surgical risks. Methods We identified a retrospective, institutional cohort of adult patients who underwent SOC for Chiari decompression between 2014 and 2023. Demographic, clinical, and radiographic features were extracted for each patient. Clinical outcomes were assessed using the Chicago Chiari Outcome Scale (CCOS) and Motor-Sensory-Sphincter signs score (Clinical Sign Score (CSS)). Radiographic outcomes assessed cerebellar ectopia and associated syrinx characteristics. Results A total of 15 patients were identified, with an average follow-up period of three years. Eight patients underwent SOC with duraplasty, whereas seven patients underwent SOC only without duraplasty. Both groups of patients were of similar age at surgery and had similar nature and duration of symptoms prior to surgery. On pre-operative radiographic evaluation, both groups of patients had similar lengths of cerebellar ectopia (9.9±11.0 mm to 11.1±5.7 mm, p=0.591), and associated syrinxes (75% vs. 42.9%, p=0.205). Intraoperatively, both groups had similar estimated blood losses, though the length of surgery was significantly shorter when durotomy was spared (202±58.3 minutes to 116.3±47.8 minutes, p=0.011). The length of ICU stay was also significantly longer in the durotomy group (1.1±0.6 days to 0.0 days, p<0.001). Neither group reported any post-operative complications. On follow-up, both groups demonstrated similar reductions in cerebellar ectopia and syrinx characteristics. Clinically, the CCOS and CSS scores were similar between the two cohorts at follow-up, with no repeat surgery required in either group. Conclusion Our cohort suggests that for adult CM1 patients, SOC decompression alone without dural reconstruction might lead to comparable clinical and radiographic outcomes to SOC decompression with durotomy/duraplasty, especially if intraoperative ultrasound confirms good cerebrospinal fluid (CSF) flow after SOC. Notably, sparing durotomy and duraplasty is also associated with decreased operative time and decreased ICU stay.
枕下颅骨切除术(SOC)联合硬脑膜切开和硬脑膜成形术用于后颅窝减压是治疗症状性Chiari 1畸形(CM1)的有效方法,主要应用于儿科患者。然而,硬脑膜切开和重建与并发症风险增加相关,其在成人患者中的必要性尚未得到有力证实。鉴于儿科和成人患者临床表现和疾病严重程度的差异,我们旨在确定仅行SOC并在术中通过超声确认小脑扁桃体搏动运动充分恢复是否足以治疗症状性CM1,同时降低手术风险。
我们确定了一个回顾性的机构队列,其中成年患者在2014年至2023年间接受了SOC进行Chiari减压。提取了每位患者的人口统计学、临床和影像学特征。使用芝加哥Chiari结局量表(CCOS)和运动-感觉-括约肌体征评分(临床体征评分(CSS))评估临床结局。影像学结局评估小脑异位和相关空洞特征。
共确定了15例患者,平均随访期为三年。8例患者接受了SOC联合硬脑膜成形术,而7例患者仅接受了SOC而未行硬脑膜成形术。两组患者手术时年龄相似,术前症状的性质和持续时间也相似。术前影像学评估显示,两组患者小脑异位的长度相似(9.9±11.0毫米至11.1±5.7毫米,p = 0.591),相关空洞的情况也相似(75%对42.9%,p = 0.205)。术中,两组估计失血量相似,但未行硬脑膜切开时手术时间明显缩短(202±58.3分钟至116.3±47.8分钟,p = 0.011)。硬脑膜切开组的重症监护病房住院时间也明显更长(1.1±0.6天至0.0天,p < 0.001)。两组均未报告任何术后并发症。随访时,两组小脑异位和空洞特征的减少情况相似。临床上,随访时两个队列的CCOS和CSS评分相似,两组均无需再次手术。
我们的队列表明,对于成年CM1患者,仅行SOC减压而不进行硬脑膜重建可能会导致与行硬脑膜切开/硬脑膜成形术的SOC减压相当的临床和影像学结局,特别是如果术中超声确认SOC后脑脊液(CSF)流动良好。值得注意的是,避免硬脑膜切开和硬脑膜成形术还与手术时间缩短和重症监护病房住院时间减少相关。